A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13029348



Internal ID2142576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154702383..154712923hg38UCSC Ensembl
Innerchr7:154702389..154712918hg38UCSC Ensembl
Outerchr7:154702378..154712929hg38UCSC Ensembl
chr7:154494093..154504633hg19UCSC Ensembl
Innerchr7:154494099..154504628hg19UCSC Ensembl
Outerchr7:154494088..154504639hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3810541
hg1910541
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615612
Supporting Variants
SamplesHG01942
Known GenesDPP6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13029348
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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